Canonical Allele Identifier: PA645494190
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319441
ClinVar RCV Id: RCV000347725 RCV001782805 RCV002261058 RCV002522857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala292Val
CA8051417
NM_022162.3:c.875C>T